Name: rs1964863
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1964863

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:2955046 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.258264 (68360/264690, TOPMED)
T=0.264039 (36900/139752, GnomAD)
T=0.25602 (7234/28256, 14KJPN) (+ 16 more)
T=0.30379 (5738/18888, ALFA)
T=0.25692 (4306/16760, 8.3KJPN)
T=0.2374 (1520/6404, 1000G_30x)
T=0.2384 (1194/5008, 1000G)
T=0.3390 (1518/4478, Estonian)
T=0.3350 (1291/3854, ALSPAC)
T=0.3484 (1292/3708, TWINSUK)
T=0.3020 (885/2930, KOREAN)
T=0.2980 (546/1832, Korea1K)
T=0.328 (327/998, GoNL)
T=0.348 (209/600, NorthernSweden)
C=0.385 (87/226, SGDP_PRJ)
T=0.407 (88/216, Qatari)
T=0.215 (46/214, Vietnamese)
C=0.36 (15/42, Siberian)
T=0.30 (12/40, GENOME_DK)

Clinical Significance: Reported in ClinVar
Gene : Consequence: SERPINB6 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	18888	C=0.69621	T=0.30379	0.490576	0.098158	0.411266	4
European	Sub	14284	C=0.66074	T=0.33926	0.436992	0.115514	0.447494	0
African	Sub	2946	C=0.8479	T=0.1521	0.717583	0.021724	0.260692	0
African Others	Sub	114	C=0.860	T=0.140	0.736842	0.017544	0.245614	0
African American	Sub	2832	C=0.8475	T=0.1525	0.716808	0.021893	0.261299	0
Asian	Sub	112	C=0.777	T=0.223	0.589286	0.035714	0.375	0
East Asian	Sub	86	C=0.74	T=0.26	0.511628	0.023256	0.465116	1
Other Asian	Sub	26	C=0.88	T=0.12	0.846154	0.076923	0.076923	3
Latin American 1	Sub	146	C=0.753	T=0.247	0.575342	0.068493	0.356164	0
Latin American 2	Sub	610	C=0.777	T=0.223	0.619672	0.065574	0.314754	2
South Asian	Sub	98	C=0.61	T=0.39	0.387755	0.163265	0.44898	0
Other	Sub	692	C=0.698	T=0.302	0.49711	0.101156	0.401734	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	C=0.741736	T=0.258264
gnomAD - Genomes	Global	Study-wide	139752	C=0.735961	T=0.264039
gnomAD - Genomes	European	Sub	75710	C=0.67517	T=0.32483
gnomAD - Genomes	African	Sub	41850	C=0.85904	T=0.14096
gnomAD - Genomes	American	Sub	13600	C=0.71324	T=0.28676
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.6547	T=0.3453
gnomAD - Genomes	East Asian	Sub	3124	C=0.7414	T=0.2586
gnomAD - Genomes	Other	Sub	2146	C=0.7423	T=0.2577
14KJPN	JAPANESE	Study-wide	28256	C=0.74398	T=0.25602
Allele Frequency Aggregator	Total	Global	18888	C=0.69621	T=0.30379
Allele Frequency Aggregator	European	Sub	14284	C=0.66074	T=0.33926
Allele Frequency Aggregator	African	Sub	2946	C=0.8479	T=0.1521
Allele Frequency Aggregator	Other	Sub	692	C=0.698	T=0.302
Allele Frequency Aggregator	Latin American 2	Sub	610	C=0.777	T=0.223
Allele Frequency Aggregator	Latin American 1	Sub	146	C=0.753	T=0.247
Allele Frequency Aggregator	Asian	Sub	112	C=0.777	T=0.223
Allele Frequency Aggregator	South Asian	Sub	98	C=0.61	T=0.39
8.3KJPN	JAPANESE	Study-wide	16760	C=0.74308	T=0.25692
1000Genomes_30x	Global	Study-wide	6404	C=0.7626	T=0.2374
1000Genomes_30x	African	Sub	1786	C=0.9009	T=0.0991
1000Genomes_30x	Europe	Sub	1266	C=0.6698	T=0.3302
1000Genomes_30x	South Asian	Sub	1202	C=0.7005	T=0.2995
1000Genomes_30x	East Asian	Sub	1170	C=0.7222	T=0.2778
1000Genomes_30x	American	Sub	980	C=0.755	T=0.245
1000Genomes	Global	Study-wide	5008	C=0.7616	T=0.2384
1000Genomes	African	Sub	1322	C=0.9032	T=0.0968
1000Genomes	East Asian	Sub	1008	C=0.7262	T=0.2738
1000Genomes	Europe	Sub	1006	C=0.6759	T=0.3241
1000Genomes	South Asian	Sub	978	C=0.706	T=0.294
1000Genomes	American	Sub	694	C=0.746	T=0.254
Genetic variation in the Estonian population	Estonian	Study-wide	4478	C=0.6610	T=0.3390
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6650	T=0.3350
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6516	T=0.3484
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.6980	T=0.3020
Korean Genome Project	KOREAN	Study-wide	1832	C=0.7020	T=0.2980
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.672	T=0.328
Northern Sweden	ACPOP	Study-wide	600	C=0.652	T=0.348
SGDP_PRJ	Global	Study-wide	226	C=0.385	T=0.615
Qatari	Global	Study-wide	216	C=0.593	T=0.407
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.785	T=0.215
Siberian	Global	Study-wide	42	C=0.36	T=0.64
The Danish reference pan genome	Danish	Study-wide	40	C=0.70	T=0.30

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 6	NC_000006.12:g.2955046C>T
GRCh37.p13 chr 6	NC_000006.11:g.2955280C>T
SERPINB6 RefSeqGene	NG_027692.1:g.22120G>A

Gene: SERPINB6, serpin family B member 6 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SERPINB6 transcript variant 2	NM_001195291.3:c.325-337G… NM_001195291.3:c.325-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 3	NM_001271822.2:c.355-337G… NM_001271822.2:c.355-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 4	NM_001271823.2:c.370-337G… NM_001271823.2:c.370-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 5	NM_001271824.2:c.313-337G… NM_001271824.2:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 6	NM_001271825.2:c.313-337G… NM_001271825.2:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 7	NM_001297699.2:c.313-337G… NM_001297699.2:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 8	NM_001297700.2:c.313-337G… NM_001297700.2:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 9	NM_001374515.1:c.325-337G… NM_001374515.1:c.325-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 10	NM_001374516.1:c.313-337G… NM_001374516.1:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 11	NM_001374517.1:c.181-337G… NM_001374517.1:c.181-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 1	NM_004568.6:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant 12	NR_164657.1:n.	N/A	Intron Variant
SERPINB6 transcript variant X2	XM_011514672.2:c.547-337G… XM_011514672.2:c.547-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X10	XM_017010941.2:c.181-337G… XM_017010941.2:c.181-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X13	XM_024446465.2:c.181-337G… XM_024446465.2:c.181-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X1	XM_047418883.1:c.547-337G… XM_047418883.1:c.547-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X3	XM_047418884.1:c.547-337G… XM_047418884.1:c.547-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X4	XM_047418885.1:c.547-337G… XM_047418885.1:c.547-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X5	XM_047418887.1:c.547-337G… XM_047418887.1:c.547-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X6	XM_047418888.1:c.547-337G… XM_047418888.1:c.547-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X7	XM_047418889.1:c.325-337G… XM_047418889.1:c.325-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X11	XM_047418890.1:c.325-337G… XM_047418890.1:c.325-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X12	XM_047418891.1:c.313-337G… XM_047418891.1:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X8	XM_047418892.1:c.313-337G… XM_047418892.1:c.313-337G>A	N/A	Intron Variant
SERPINB6 transcript variant X9	XM_047418893.1:c.181-337G… XM_047418893.1:c.181-337G>A	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: T (allele ID: 1278533 )

ClinVar Accession	Disease Names	Clinical Significance
RCV001709148.1	not provided	Benign

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	C=	T
GRCh38.p14 chr 6	NC_000006.12:g.2955046=	NC_000006.12:g.2955046C>T
GRCh37.p13 chr 6	NC_000006.11:g.2955280=	NC_000006.11:g.2955280C>T
SERPINB6 RefSeqGene	NG_027692.1:g.22120=	NG_027692.1:g.22120G>A
SERPINB6 transcript variant 2	NM_001195291.2:c.325-337=	NM_001195291.2:c.325-337G>A
SERPINB6 transcript variant 2	NM_001195291.3:c.325-337=	NM_001195291.3:c.325-337G>A
SERPINB6 transcript variant 3	NM_001271822.1:c.355-337=	NM_001271822.1:c.355-337G>A
SERPINB6 transcript variant 3	NM_001271822.2:c.355-337=	NM_001271822.2:c.355-337G>A
SERPINB6 transcript variant 4	NM_001271823.1:c.370-337=	NM_001271823.1:c.370-337G>A
SERPINB6 transcript variant 4	NM_001271823.2:c.370-337=	NM_001271823.2:c.370-337G>A
SERPINB6 transcript variant 5	NM_001271824.1:c.313-337=	NM_001271824.1:c.313-337G>A
SERPINB6 transcript variant 5	NM_001271824.2:c.313-337=	NM_001271824.2:c.313-337G>A
SERPINB6 transcript variant 6	NM_001271825.1:c.313-337=	NM_001271825.1:c.313-337G>A
SERPINB6 transcript variant 6	NM_001271825.2:c.313-337=	NM_001271825.2:c.313-337G>A
SERPINB6 transcript variant 7	NM_001297699.2:c.313-337=	NM_001297699.2:c.313-337G>A
SERPINB6 transcript variant 8	NM_001297700.2:c.313-337=	NM_001297700.2:c.313-337G>A
SERPINB6 transcript variant 9	NM_001374515.1:c.325-337=	NM_001374515.1:c.325-337G>A
SERPINB6 transcript variant 10	NM_001374516.1:c.313-337=	NM_001374516.1:c.313-337G>A
SERPINB6 transcript variant 11	NM_001374517.1:c.181-337=	NM_001374517.1:c.181-337G>A
SERPINB6 transcript variant 1	NM_004568.5:c.313-337=	NM_004568.5:c.313-337G>A
SERPINB6 transcript variant 1	NM_004568.6:c.313-337=	NM_004568.6:c.313-337G>A
SERPINB6 transcript variant X1	XM_005249181.1:c.412-337=	XM_005249181.1:c.412-337G>A
SERPINB6 transcript variant X2	XM_005249182.1:c.313-337=	XM_005249182.1:c.313-337G>A
SERPINB6 transcript variant X3	XM_005249183.1:c.46-337=	XM_005249183.1:c.46-337G>A
SERPINB6 transcript variant X2	XM_011514672.2:c.547-337=	XM_011514672.2:c.547-337G>A
SERPINB6 transcript variant X10	XM_017010941.2:c.181-337=	XM_017010941.2:c.181-337G>A
SERPINB6 transcript variant X13	XM_024446465.2:c.181-337=	XM_024446465.2:c.181-337G>A
SERPINB6 transcript variant X1	XM_047418883.1:c.547-337=	XM_047418883.1:c.547-337G>A
SERPINB6 transcript variant X3	XM_047418884.1:c.547-337=	XM_047418884.1:c.547-337G>A
SERPINB6 transcript variant X4	XM_047418885.1:c.547-337=	XM_047418885.1:c.547-337G>A
SERPINB6 transcript variant X5	XM_047418887.1:c.547-337=	XM_047418887.1:c.547-337G>A
SERPINB6 transcript variant X6	XM_047418888.1:c.547-337=	XM_047418888.1:c.547-337G>A
SERPINB6 transcript variant X7	XM_047418889.1:c.325-337=	XM_047418889.1:c.325-337G>A
SERPINB6 transcript variant X11	XM_047418890.1:c.325-337=	XM_047418890.1:c.325-337G>A
SERPINB6 transcript variant X12	XM_047418891.1:c.313-337=	XM_047418891.1:c.313-337G>A
SERPINB6 transcript variant X8	XM_047418892.1:c.313-337=	XM_047418892.1:c.313-337G>A
SERPINB6 transcript variant X9	XM_047418893.1:c.181-337=	XM_047418893.1:c.181-337G>A

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

59 SubSNP, 19 Frequency, 1 ClinVar submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss2868207	Jan 12, 2001 (92)
2	YUSUKE	ss5009554	Aug 28, 2002 (126)
3	SC_JCM	ss5891128	Feb 20, 2003 (111)
4	BCM_SSAHASNP	ss10287307	Jul 11, 2003 (116)
5	SSAHASNP	ss22484043	Apr 05, 2004 (121)
6	ABI	ss42792522	Mar 11, 2006 (126)
7	HUMANGENOME_JCVI	ss98361178	Feb 06, 2009 (130)
8	ENSEMBL	ss143951370	Dec 01, 2009 (131)
9	GMI	ss156453499	Dec 01, 2009 (131)
10	COMPLETE_GENOMICS	ss161966100	Jul 04, 2010 (132)
11	COMPLETE_GENOMICS	ss163063082	Jul 04, 2010 (132)
12	COMPLETE_GENOMICS	ss166030444	Jul 04, 2010 (132)
13	BL	ss253989429	May 09, 2011 (134)
14	GMI	ss278626747	May 04, 2012 (137)
15	PJP	ss293584968	May 09, 2011 (134)
16	1000GENOMES	ss333041168	May 09, 2011 (134)
17	TISHKOFF	ss558958213	Apr 25, 2013 (138)
18	SSMP	ss652870094	Apr 25, 2013 (138)
19	EVA-GONL	ss982515945	Aug 21, 2014 (142)
20	JMKIDD_LAB	ss1073329492	Aug 21, 2014 (142)
21	1000GENOMES	ss1318718009	Aug 21, 2014 (142)
22	EVA_GENOME_DK	ss1581504472	Apr 01, 2015 (144)
23	EVA_DECODE	ss1592061573	Apr 01, 2015 (144)
24	EVA_UK10K_ALSPAC	ss1614811422	Apr 01, 2015 (144)
25	EVA_UK10K_TWINSUK	ss1657805455	Apr 01, 2015 (144)
26	WEILL_CORNELL_DGM	ss1925773211	Feb 12, 2016 (147)
27	JJLAB	ss2023501132	Sep 14, 2016 (149)
28	USC_VALOUEV	ss2151663052	Dec 20, 2016 (150)
29	HUMAN_LONGEVITY	ss2281271948	Dec 20, 2016 (150)
30	SYSTEMSBIOZJU	ss2626238875	Nov 08, 2017 (151)
31	GRF	ss2707247768	Nov 08, 2017 (151)
32	GNOMAD	ss2835087679	Nov 08, 2017 (151)
33	SWEGEN	ss2998412209	Nov 08, 2017 (151)
34	BIOINF_KMB_FNS_UNIBA	ss3025534029	Nov 08, 2017 (151)
35	CSHL	ss3346804506	Nov 08, 2017 (151)
36	URBANLAB	ss3648253373	Oct 12, 2018 (152)
37	EGCUT_WGS	ss3666335260	Jul 13, 2019 (153)
38	EVA_DECODE	ss3716454993	Jul 13, 2019 (153)
39	ACPOP	ss3733145458	Jul 13, 2019 (153)
40	EVA	ss3764532032	Jul 13, 2019 (153)
41	KHV_HUMAN_GENOMES	ss3807692916	Jul 13, 2019 (153)
42	EVA	ss3829696564	Apr 26, 2020 (154)
43	EVA	ss3838322768	Apr 26, 2020 (154)
44	EVA	ss3843762581	Apr 26, 2020 (154)
45	SGDP_PRJ	ss3863782877	Apr 26, 2020 (154)
46	KRGDB	ss3910516388	Apr 26, 2020 (154)
47	KOGIC	ss3958375449	Apr 26, 2020 (154)
48	TOPMED	ss4691574322	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5175874574	Apr 26, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5267175950	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5464990648	Oct 13, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5552497133	Oct 13, 2022 (156)
53	SANFORD_IMAGENETICS	ss5639637784	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5713458447	Oct 13, 2022 (156)
55	YY_MCH	ss5807095237	Oct 13, 2022 (156)
56	EVA	ss5841703751	Oct 13, 2022 (156)
57	EVA	ss5855173830	Oct 13, 2022 (156)
58	EVA	ss5882395786	Oct 13, 2022 (156)
59	EVA	ss5968130776	Oct 13, 2022 (156)
60	1000Genomes	NC_000006.11 - 2955280	Oct 12, 2018 (152)
61	1000Genomes_30x	NC_000006.12 - 2955046	Oct 13, 2022 (156)
62	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 2955280	Oct 12, 2018 (152)
63	Genetic variation in the Estonian population	NC_000006.11 - 2955280	Oct 12, 2018 (152)
64	The Danish reference pan genome	NC_000006.11 - 2955280	Apr 26, 2020 (154)
65	gnomAD - Genomes	NC_000006.12 - 2955046	Apr 26, 2021 (155)
66	Genome of the Netherlands Release 5	NC_000006.11 - 2955280	Apr 26, 2020 (154)
67	KOREAN population from KRGDB	NC_000006.11 - 2955280	Apr 26, 2020 (154)
68	Korean Genome Project	NC_000006.12 - 2955046	Apr 26, 2020 (154)
69	Northern Sweden	NC_000006.11 - 2955280	Jul 13, 2019 (153)
70	Qatari	NC_000006.11 - 2955280	Apr 26, 2020 (154)
71	SGDP_PRJ	NC_000006.11 - 2955280	Apr 26, 2020 (154)
72	Siberian	NC_000006.11 - 2955280	Apr 26, 2020 (154)
73	8.3KJPN	NC_000006.11 - 2955280	Apr 26, 2021 (155)
74	14KJPN	NC_000006.12 - 2955046	Oct 13, 2022 (156)
75	TopMed	NC_000006.12 - 2955046	Apr 26, 2021 (155)
76	UK 10K study - Twins	NC_000006.11 - 2955280	Oct 12, 2018 (152)
77	A Vietnamese Genetic Variation Database	NC_000006.11 - 2955280	Jul 13, 2019 (153)
78	ALFA	NC_000006.12 - 2955046	Apr 26, 2021 (155)
79	ClinVar	RCV001709148.1	Oct 13, 2022 (156)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs3823092	Mar 11, 2006 (126)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss161966100, ss163063082, ss166030444, ss253989429, ss278626747, ss293584968, ss1592061573	NC_000006.10:2900278:C:T	NC_000006.12:2955045:C:T	(self)
30450432, 16948588, 12073508, 7669411, 7522896, 17693782, 6430323, 7815141, 15799857, 4179406, 33843881, 16948588, 3753724, ss333041168, ss558958213, ss652870094, ss982515945, ss1073329492, ss1318718009, ss1581504472, ss1614811422, ss1657805455, ss1925773211, ss2023501132, ss2151663052, ss2626238875, ss2707247768, ss2835087679, ss2998412209, ss3346804506, ss3666335260, ss3733145458, ss3764532032, ss3829696564, ss3838322768, ss3863782877, ss3910516388, ss5175874574, ss5639637784, ss5841703751, ss5968130776	NC_000006.11:2955279:C:T	NC_000006.12:2955045:C:T	(self)
RCV001709148.1, 40023068, 215319565, 14753450, 47295551, 528951880, 1973730504, ss2281271948, ss3025534029, ss3648253373, ss3716454993, ss3807692916, ss3843762581, ss3958375449, ss4691574322, ss5267175950, ss5464990648, ss5552497133, ss5713458447, ss5807095237, ss5855173830, ss5882395786	NC_000006.12:2955045:C:T	NC_000006.12:2955045:C:T	(self)
ss2868207, ss5009554, ss5891128, ss42792522, ss98361178, ss143951370, ss156453499	NT_007592.15:2895279:C:T	NC_000006.12:2955045:C:T	(self)
ss10287307	NT_034880.2:2895278:C:T	NC_000006.12:2955045:C:T	(self)
ss22484043	NT_034880.3:2895278:C:T	NC_000006.12:2955045:C:T	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1964863

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1964863